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#S22;(S)-3-[5-[4-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-

Compound with spectra: 1 NMR

#S22;(S)-3-[5-[4-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-
SpectraBase Compound ID GDLr2VACzTL
InChI InChI=1S/C39H40F20N4O4SSi/c1-22(2)69(23(3)4,16-13-31(40,41)32(42,43)33(44,45)34(46,47)35(48,49)36(50,51)37(52,53)38(54,55)56)67-21-24-9-11-25(12-10-24)29-17-27(20-63(29)68(65,66)39(57,58)59)26-7-6-15-62(19-26)30(64)61-28-8-5-14-60-18-28/h5,7-12,14,17-18,22-23,29H,6,13,15-16,19-21H2,1-4H3,(H,61,64)/t29-/m0/s1
InChIKey VDJUVRUKXNIPRP-LJAQVGFWSA-N
Mol Weight 1068.9 g/mol
Molecular Formula C39H40F20N4O4SSi
Exact Mass 1068.222017 g/mol
Enantiomer InChIKey VDJUVRUKXNIPRP-GDLZYMKVSA-N
Racemate InChIKey VDJUVRUKXNIPRP-UHFFFAOYSA-N

View Spectrum of #S22;(S)-3-[5-[4-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H-

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#S23;(S)-[3-[5-[4-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-PHENYL]-1-(TRIFLUOROMETHYLSULFONYL)-2,5-DIHYDRO-1H
#S9;[(1R,4S)-4-[[N-[(S)-1-[4-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-PHENYL]-ALLYL]-2-NITROPHENYLSULFONAMIDO
#S18;(R)-2-[[(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-HEPTADECAFLUORODECYL)-DIISOPROPYLSILYLOXY]-METHYL]-1-(2-NITROPHENYLSULFONYL)-5-[(1,1,1-TRIFLUOROMETHYLSULFON
17-.Benzoyl-3-methoxyestra-1,3,510),16-tetraene
6-DEOXY-1,2:3,4-DI-O-ISOPROPYLIDENE-6-C-[METHYL-(E)-2,3,4-TRI-O-BENZYL-7-DEOXY-ALPHA-D-GLUCO-HEPTOPYRANOSID-6-ULOS-7-YLIDENE]-ALPHA-D-
ENT-2,3-SECOBEYER-15-ENE-2,3-DIOIC-ACID-DIMETHYLESTER
5-(2-Chloroethyl)-3-(4-chlorophenyl)-6-methyl-1-phenyl-1,7-dihydro-4H-pyrazolo[3,4-b]pyridin-4-one
(E)-1-(4-BROMO-3-METHYLBUT-2-ENYL)-3-(2-METHYLBUT-3-EN-2-OLYL)-6,7-DIMETHOXYQUINAZOLINE-2,4-(1H,3H)-DIONE
CONFERTIFOLINE,7-A-CHLORO-6-OXO
No Name
Title Journal or Book Year
Synthesis of skeletally diverse alkaloid-like molecules: exploitation of metathesis substrates assembled from triplets of building blocks Beilstein Journal of Organic Chemistry 2013
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